Spinal muscular atrophy (SMA) is a genetic lower motor neuron disease. It usually involves all of the skeletal muscles innervated by the anterior horn cells of the spinal cord. In rare cases, there is also localised involvement of the spinal cord. We report a 10-year-old boy who presented to the Sultan Qaboos University Hospital, Muscat, Oman, in 2015 with muscle weakness restricted to the lower limbs. The presence of a homozygous deletion within the survival of motor neuron 1 gene confirmed the diagnosis of SMA. To the best of the authors’ knowledge, this is the first report of an Omani patient with segmental SMA involving only the lower limbs. Treatment for this rare and relatively benign form of SMA is symptomatic and includes physiother...
The transposition of the great arteries (TGA) is a complex congenital heart disease which usually pr...
To this day, tuberculosis (TB) continues to pose a significant global health burden. The World Healt...
Sickle cell disease and homozygous β-thalassaemia are common haemoglobinopathies in Oman, with many ...
Acute polyneuropathy is a rare manifestation of severe hyperthyroidism. We report a 22-year-old Oman...
Congenital contractural arachnodactyly, commonly known as Beal’s syndrome, is an extremely rare gene...
Tyrosine hydroxylase (TH) deficiency is a rare autosomal recessive and often treatable neurometaboli...
Squamous cell carcinoma (SCC) of the endometrium, whether primary or secondary to cervical cancer, i...
Oedema refers to the excessive accumulation of fluid within intercellular tissues as a result of dis...
Sickle cell anaemia (SCA) is a common haemoglobinopathy among people from the Middle East, the Afro-...
Because of their physical size and physiological immaturity, resuscitation of extremely very low bir...
Eating epilepsy (EE), where seizures are triggered by eating, is rare and has not been reported in t...
A salivary gland anlage tumour (SGAT) is a very rare type of benign tumour that usually presents in ...
Acne vulgaris is one of the most common chronic inflammatory skin disorders among adolescents and yo...
An undifferentiated embryonal sarcoma of the liver is a rare malignant tumour. We highlight the diag...
Gastric intubation is a common and simple procedure that is often performed on patients who are seda...
The transposition of the great arteries (TGA) is a complex congenital heart disease which usually pr...
To this day, tuberculosis (TB) continues to pose a significant global health burden. The World Healt...
Sickle cell disease and homozygous β-thalassaemia are common haemoglobinopathies in Oman, with many ...
Acute polyneuropathy is a rare manifestation of severe hyperthyroidism. We report a 22-year-old Oman...
Congenital contractural arachnodactyly, commonly known as Beal’s syndrome, is an extremely rare gene...
Tyrosine hydroxylase (TH) deficiency is a rare autosomal recessive and often treatable neurometaboli...
Squamous cell carcinoma (SCC) of the endometrium, whether primary or secondary to cervical cancer, i...
Oedema refers to the excessive accumulation of fluid within intercellular tissues as a result of dis...
Sickle cell anaemia (SCA) is a common haemoglobinopathy among people from the Middle East, the Afro-...
Because of their physical size and physiological immaturity, resuscitation of extremely very low bir...
Eating epilepsy (EE), where seizures are triggered by eating, is rare and has not been reported in t...
A salivary gland anlage tumour (SGAT) is a very rare type of benign tumour that usually presents in ...
Acne vulgaris is one of the most common chronic inflammatory skin disorders among adolescents and yo...
An undifferentiated embryonal sarcoma of the liver is a rare malignant tumour. We highlight the diag...
Gastric intubation is a common and simple procedure that is often performed on patients who are seda...
The transposition of the great arteries (TGA) is a complex congenital heart disease which usually pr...
To this day, tuberculosis (TB) continues to pose a significant global health burden. The World Healt...
Sickle cell disease and homozygous β-thalassaemia are common haemoglobinopathies in Oman, with many ...